Canonical Allele Identifier: CA2148395974

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77441508_77441509delinsAC , CM000676.2:g.77441508_77441509delinsAC	GRCh38
NC_000014.8:g.77907851_77907852delinsAC , CM000676.1:g.77907851_77907852delinsAC	GRCh37
NC_000014.7:g.76977604_76977605delinsAC	NCBI36
NG_023421.1:g.21132_21133delinsGT
NG_023421.2:g.21132_21133delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557658.6:c.735-416_735-415delinsGT MANE Select	ENSP00000452191.1:n.735-416_735-415delinsGT
ENST00000327028.8:c.588-416_588-415delinsGT	ENSP00000313098.5:n.588-416_588-415delinsGT
ENST00000343765.6:c.735-416_735-415delinsGT	ENSP00000339122.2:n.735-416_735-415delinsGT
ENST00000448935.6:c.588-416_588-415delinsGT	ENSP00000404815.2:n.588-416_588-415delinsGT
ENST00000553576.5:n.147-416_147-415delinsGT
ENST00000553691.5:n.625-336_625-335delinsGT
ENST00000553888.5:c.735-416_735-415delinsGT	ENSP00000452181.1:n.735-416_735-415delinsGT
ENST00000555854.1:n.180-416_180-415delinsGT
ENST00000556412.4:c.813-416_813-415delinsGT	ENSP00000451857.1:n.813-416_813-415delinsGT
ENST00000557658.5:c.735-416_735-415delinsGT	ENSP00000452191.1:n.735-416_735-415delinsGT
NM_001193314.1:c.735-416_735-415delinsGT	NP_001180243.1:n.735-416_735-415delinsGT
NM_001193315.1:c.735-416_735-415delinsGT	NP_001180244.1:n.735-416_735-415delinsGT
NM_001193316.1:c.588-416_588-415delinsGT	NP_001180245.1:n.588-416_588-415delinsGT
NM_001193317.1:c.735-416_735-415delinsGT	NP_001180246.1:n.735-416_735-415delinsGT
NM_022067.3:c.735-416_735-415delinsGT	NP_071350.2:n.735-416_735-415delinsGT
XM_011537066.1:c.642-416_642-415delinsGT	XP_011535368.1:n.642-416_642-415delinsGT
XM_011537066.2:c.642-416_642-415delinsGT	XP_011535368.1:n.642-416_642-415delinsGT
XM_017021580.2:c.735-416_735-415delinsGT	XP_016877069.1:n.735-416_735-415delinsGT
XM_017021581.2:c.735-416_735-415delinsGT	XP_016877070.1:n.735-416_735-415delinsGT
XM_024449688.1:c.642-416_642-415delinsGT	XP_024305456.1:n.642-416_642-415delinsGT
XR_001750501.2:n.857-416_857-415delinsGT
NM_001193314.2:c.735-416_735-415delinsGT	NP_001180243.1:n.735-416_735-415delinsGT
NM_001193316.2:c.588-416_588-415delinsGT	NP_001180245.1:n.588-416_588-415delinsGT
NM_001193317.2:c.735-416_735-415delinsGT	NP_001180246.1:n.735-416_735-415delinsGT
NM_022067.4:c.735-416_735-415delinsGT	NP_071350.2:n.735-416_735-415delinsGT
NM_001193315.2:c.735-416_735-415delinsGT MANE Select	NP_001180244.1:n.735-416_735-415delinsGT
NM_001400324.1:c.588-416_588-415delinsGT	NP_001387253.1:n.588-416_588-415delinsGT
NM_001400325.1:c.588-416_588-415delinsGT	NP_001387254.1:n.588-416_588-415delinsGT
NM_001400326.1:c.735-416_735-415delinsGT	NP_001387255.1:n.735-416_735-415delinsGT
NM_001400327.1:c.702-416_702-415delinsGT	NP_001387256.1:n.702-416_702-415delinsGT
NM_001400330.1:c.735-416_735-415delinsGT	NP_001387259.1:n.735-416_735-415delinsGT
NM_001400331.1:c.735-416_735-415delinsGT	NP_001387260.1:n.735-416_735-415delinsGT
NM_001400332.1:c.735-416_735-415delinsGT	NP_001387261.1:n.735-416_735-415delinsGT
NM_001400333.1:c.642-416_642-415delinsGT	NP_001387262.1:n.642-416_642-415delinsGT
NM_001400334.1:c.642-416_642-415delinsGT	NP_001387263.1:n.642-416_642-415delinsGT
NM_001400335.1:c.735-416_735-415delinsGT	NP_001387264.1:n.735-416_735-415delinsGT
NM_001400336.1:c.735-416_735-415delinsGT	NP_001387265.1:n.735-416_735-415delinsGT
NM_001400337.1:c.495-416_495-415delinsGT	NP_001387266.1:n.495-416_495-415delinsGT
NM_001400338.1:c.734+1051_734+1052delinsGT	NP_001387267.1:n.734+1051_734+1052delinsGT
NM_001400339.1:c.735-416_735-415delinsGT	NP_001387268.1:n.735-416_735-415delinsGT
NR_174476.1:n.842-416_842-415delinsGT